MiMeDB: Showing metabocard for 3-(Imidazol-4-yl)-2-oxopropyl phosphate (MMDBc0049988)

Record Information

Version

2.0

Status

Detected and Quantified

Creation Date

2022-04-29 22:47:41 UTC

Update Date

2025-01-15 23:10:54 UTC

Metabolite ID

MMDBc0049988

Metabolite Identification

Common Name

3-(Imidazol-4-yl)-2-oxopropyl phosphate

Description

Imidazole acetol-phosphate is involved in the histidine biosynthesis I pathway. Imidazole acetol-phosphate is created by the breakdown of D-erythro-imidazole-glycerol-phosphate into imidazole acetol-phosphate and H2O. Imidazoleglycerol-phosphate dehydratase catalyzes this reaction. Imidazole acetol-phosphate reacts with L-glutamate to produce L-histidinol-phosphate and 2-ketoglutarate. Histidinol-phosphate aminotransferase catalyzes this reaction.

Structure

MOL 3D MOL SDF 3D SDF PDB 3D PDB SMILES InChI


  Mrv1652309042000352D          

 14 14  0  0  0  0            999 V2000
 9999.234510000.2470    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9999.9491 9999.8348    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10000.662910000.2470    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9999.9491 9999.0097    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10001.3781 9999.8348    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10002.093410000.2470    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
10001.681110000.9602    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10002.8065 9999.8348    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10002.505610000.9602    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 9997.848210000.3289    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
 9997.1808 9999.8439    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9997.4357 9999.0593    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
 9998.2607 9999.0593    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9998.5156 9999.8439    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  2  4  2  0  0  0  0
  3  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  6  8  1  0  0  0  0
  6  9  1  0  0  0  0
 13 14  2  0  0  0  0
 10 11  2  0  0  0  0
 10 14  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
  1 14  1  0  0  0  0
M  END
> <DATABASE_ID>
MMDBc0049988

> <DATABASE_NAME>
MIME

> <SMILES>
OP(O)(=O)OCC(=O)CC1=CNC=N1

> <INCHI_IDENTIFIER>
InChI=1S/C6H9N2O5P/c9-6(3-13-14(10,11)12)1-5-2-7-4-8-5/h2,4H,1,3H2,(H,7,8)(H2,10,11,12)

> <INCHI_KEY>
YCFFMSOLUMRAMD-UHFFFAOYSA-N

> <FORMULA>
C6H9N2O5P

> <MOLECULAR_WEIGHT>
220.1198

> <EXACT_MASS>
220.02490792

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_ATOM_COUNT>
23

> <JCHEM_AVERAGE_POLARIZABILITY>
18.148917277754943

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
[3-(1H-imidazol-4-yl)-2-oxopropoxy]phosphonic acid

> <ALOGPS_LOGP>
-0.90

> <JCHEM_LOGP>
-2.9574821134456775

> <ALOGPS_LOGS>
-1.17

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-2

> <JCHEM_PKA>
6.03139600175535

> <JCHEM_PKA_STRONGEST_ACIDIC>
1.2314915163527376

> <JCHEM_PKA_STRONGEST_BASIC>
6.647396425017994

> <JCHEM_POLAR_SURFACE_AREA>
112.51

> <JCHEM_REFRACTIVITY>
46.0746

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.49e+01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
3-(1H-imidazol-4-yl)-2-oxopropoxyphosphonic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 04-SEP-20   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   04-SEP-20         0                                  
HETATM    1  C   UNK     0    8665.2388667.128   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0    8666.5728666.358   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0    8667.9048667.128   0.000  0.00  0.00           C+0
HETATM    4  O   UNK     0    8666.5728664.818   0.000  0.00  0.00           O+0
HETATM    5  O   UNK     0    8669.2398666.358   0.000  0.00  0.00           O+0
HETATM    6  P   UNK     0    8670.5748667.128   0.000  0.00  0.00           P+0
HETATM    7  O   UNK     0    8669.8058668.459   0.000  0.00  0.00           O+0
HETATM    8  O   UNK     0    8671.9058666.358   0.000  0.00  0.00           O+0
HETATM    9  O   UNK     0    8671.3448668.459   0.000  0.00  0.00           O+0
HETATM   10  N   UNK     0    8662.6508667.281   0.000  0.00  0.00           N+0
HETATM   11  C   UNK     0    8661.4048666.375   0.000  0.00  0.00           C+0
HETATM   12  N   UNK     0    8661.8808664.911   0.000  0.00  0.00           N+0
HETATM   13  C   UNK     0    8663.4208664.911   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0    8663.8968666.375   0.000  0.00  0.00           C+0
CONECT    1    2   14                                                       
CONECT    2    1    3    4                                                  
CONECT    3    2    5                                                       
CONECT    4    2                                                            
CONECT    5    3    6                                                       
CONECT    6    5    7    8    9                                             
CONECT    7    6                                                            
CONECT    8    6                                                            
CONECT    9    6                                                            
CONECT   10   11   14                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13                                                       
CONECT   13   14   12                                                       
CONECT   14   13   10    1                                                  
MASTER        0    0    0    0    0    0    0    0   14    0   28    0
END

Synonyms

Value	Source
3-(Imidazol-4-yl)-2-oxopropyl phosphate	ChEBI
Imidazole-acetol phosphate	ChEBI
3-(Imidazol-4-yl)-2-oxopropyl phosphoric acid	Generator
Imidazole-acetol phosphoric acid	Generator
Imidazole acetol-phosphoric acid	Generator
1-(1H-Imidazol-4-yl)-3-(phosphonooxy)-2-propanone	HMDB
3-(1H-Imidazol-4-yl)-2-oxopropyl dihydrogen phosphate	HMDB
3-(Imidazol-4-yl)-2-oxopropyl dihydrogen phosphate	HMDB
Imidazole acetol phosphate	HMDB
Imidazole acetol-P	HMDB
1-(1H-Imidazol-5-yl)-3-(phosphonooxy)-2-propanone	HMDB

Molecular Formula

C₆H₉N₂O₅P

Average Mass

220.1198

Monoisotopic Mass

220.02490792

IUPAC Name

[3-(1H-imidazol-4-yl)-2-oxopropoxy]phosphonic acid

Traditional Name

3-(1H-imidazol-4-yl)-2-oxopropoxyphosphonic acid

CAS Registry Number

Not Available

SMILES

OP(O)(=O)OCC(=O)CC1=CNC=N1

InChI Identifier

InChI=1S/C6H9N2O5P/c9-6(3-13-14(10,11)12)1-5-2-7-4-8-5/h2,4H,1,3H2,(H,7,8)(H2,10,11,12)

InChI Key

YCFFMSOLUMRAMD-UHFFFAOYSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as monoalkyl phosphates. These are organic compounds containing a phosphate group that is linked to exactly one alkyl chain.

Kingdom

Organic compounds

Super Class

Organic acids and derivatives

Class

Organic phosphoric acids and derivatives

Sub Class

Phosphate esters

Direct Parent

Monoalkyl phosphates

Alternative Parents

Substituents

Monoalkyl phosphate
Azole
Imidazole
Heteroaromatic compound
Ketone
Organoheterocyclic compound
Azacycle
Organic oxide
Organooxygen compound
Organonitrogen compound
Organopnictogen compound
Organic oxygen compound
Carbonyl group
Organic nitrogen compound
Hydrocarbon derivative
Aromatic heteromonocyclic compound

Molecular Framework

Aromatic heteromonocyclic compounds

External Descriptors

imidazoles (CHEBI:16426 )
oxoalkyl phosphate (CHEBI:16426 )

Functional Ontology

Not Available

Physical Properties

State

Solid

Predicted Properties

Property	Value	Source
Water Solubility	14.9 g/L	ALOGPS
logP	-0.9	ALOGPS
logP	-3	ChemAxon
logS	-1.2	ALOGPS
pKa (Strongest Acidic)	1.23	ChemAxon
pKa (Strongest Basic)	6.65	ChemAxon
Physiological Charge	-2	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	112.51 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	46.07 m³·mol⁻¹	ChemAxon
Polarizability	18.15 Å³	ChemAxon
Number of Rings	1	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

Spectra

Spectrum Type	Description	Splash Key	Deposition Date	View
Predicted GC-MS	Predicted GC-MS Spectrum - GC-MS (Non-derivatized) - 70eV, Positive	splash10-000t-9200000000-41a681dee161ad4f3e7b	2016-09-22	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - GC-MS (Non-derivatized) - 70eV, Positive	Not Available	2021-10-12	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Positive	splash10-0fk9-3390000000-102fb9b517f2001e0996	2015-09-15	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Positive	splash10-0kmi-4950000000-076be23324f875b841dc	2015-09-15	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Positive	splash10-0a59-9500000000-99bd6a8eac665bc00868	2015-09-15	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Negative	splash10-016r-7190000000-c52bfb05c2cd90023536	2015-09-15	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Negative	splash10-004i-9000000000-7598c15214a6b2b67038	2015-09-15	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Negative	splash10-004i-9000000000-59a5e26dad504ee2412d	2015-09-15	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Positive	splash10-00di-0090000000-199895f882e036c55087	2021-09-22	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Positive	splash10-00di-3930000000-3a2cf619e974119e8f24	2021-09-22	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Positive	splash10-0pw9-9300000000-f31212a9e65f18dabcb3	2021-09-22	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Negative	splash10-014i-2090000000-bd2937021ad7bda9fa53	2021-09-23	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Negative	splash10-004i-9020000000-af7370fa1a56f74a6fb4	2021-09-23	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Negative	splash10-004i-9000000000-8c5fbfcdabecdcd6d55b	2021-09-23	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)		2021-09-29	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, D₂O, predicted)		2021-09-29	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)		2021-09-29	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, D₂O, predicted)		2021-09-29	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)		2021-09-29	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, D₂O, predicted)		2021-09-29	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)		2021-09-29	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, D₂O, predicted)		2021-09-29	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)		2021-09-29	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, D₂O, predicted)		2021-09-29	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)		2021-09-29	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, D₂O, predicted)		2021-09-29	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)		2021-09-29	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, D₂O, predicted)		2021-09-29	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)		2021-09-29	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, D₂O, predicted)		2021-09-29	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)		2021-09-29	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, D₂O, predicted)		2021-09-29	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, predicted)		2021-09-29	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, D₂O, predicted)		2021-09-29	View Spectrum

Chromatographic Retention Times and Retention Indices

Retention Times

Chromatography Type	Technique	Column	Deposition Date	Retention Time (s)
Liquid Chromatography	HILIC	Waters Acquity UPLC-BEH Amide column (eluted)	2025-10-24	455.9
Liquid Chromatography	HILIC	Waters Acquity UPLC-BEH Amide column (eluted)	2025-10-24	455.9
Liquid Chromatography	HILIC	Accucore 150 Amide HILIC (eluted)	2025-10-24	398.1
Liquid Chromatography	HILIC	Accucore 150 Amide HILIC (eluted)	2025-10-24	398.1
Liquid Chromatography	Reversed-phase	Hypersil Gold 1.9 µm C18 (void)	2025-10-24	38.5
Liquid Chromatography	Reversed-phase	Hypersil Gold 1.9 µm C18 (void)	2025-10-24	38.5
Liquid Chromatography	Reversed-phase	Agilent Zorbax Eclipse Plus C18 (2.1 mm x 150 mm, 3.5 um) (eluted)	2025-10-24	226.6
Liquid Chromatography	Reversed-phase	Agilent Zorbax Eclipse Plus C18 (2.1 mm x 150 mm, 3.5 um) (eluted)	2025-10-24	226.6
Liquid Chromatography	Reversed-phase	XBridge C18 3.5u 2.1x50 mm (eluted)	2025-10-24	278.2
Liquid Chromatography	Reversed-phase	XBridge C18 3.5u 2.1x50 mm (eluted)	2025-10-24	278.2
Liquid Chromatography	Reversed-phase	Ascentis Express C18 (void)	2025-10-24	273.2
Liquid Chromatography	Reversed-phase	Ascentis Express C18 (void)	2025-10-24	273.2
Liquid Chromatography	Reversed-phase	Waters ACQUITY UPLC HSS T3 C18 (eluted)	2025-10-24	380.7
Liquid Chromatography	Reversed-phase	Waters ACQUITY UPLC HSS T3 C18 (eluted)	2025-10-24	380.7
Liquid Chromatography	HILIC	Merck SeQuant ZIC-HILIC (eluted)	2025-10-24	880.0
Liquid Chromatography	HILIC	Merck SeQuant ZIC-HILIC (eluted)	2025-10-24	880.0
Liquid Chromatography	HILIC	Merck SeQuant ZIC-pHILIC (eluted)	2025-10-24	630.7
Liquid Chromatography	HILIC	Merck SeQuant ZIC-pHILIC (eluted)	2025-10-24	630.7
Liquid Chromatography	Reversed-phase	Waters ACQUITY UPLC HSS T3 C18 (eluted)	2025-10-24	165.7
Liquid Chromatography	Reversed-phase	Waters ACQUITY UPLC HSS T3 C18 (eluted)	2025-10-24	165.7
Liquid Chromatography	HILIC	Merck SeQuant ZIC-HILIC (eluted)	2025-10-24	513.1
Liquid Chromatography	HILIC	Merck SeQuant ZIC-HILIC (eluted)	2025-10-24	513.1
Liquid Chromatography	Reversed-phase	Waters ACQUITY UPLC HSS T3 C18 (eluted)	2025-10-24	174.7
Liquid Chromatography	Reversed-phase	Waters ACQUITY UPLC HSS T3 C18 (eluted)	2025-10-24	174.7
Liquid Chromatography	Reversed-phase	Waters ACQUITY UPLC BEH C18 (eluted)	2025-10-24	40.4
Liquid Chromatography	Reversed-phase	Waters ACQUITY UPLC BEH C18 (eluted)	2025-10-24	40.4
Liquid Chromatography	HILIC	Merck SeQuant ZIC-pHILIC column (eluted)	2025-10-24	397.3
Liquid Chromatography	HILIC	Merck SeQuant ZIC-pHILIC column (eluted)	2025-10-24	397.3
Liquid Chromatography	HILIC	Merck SeQuant ZIC-pHILIC column (eluted)	2025-10-24	771.2
Liquid Chromatography	HILIC	Merck SeQuant ZIC-pHILIC column (eluted)	2025-10-24	771.2
Liquid Chromatography	Reversed-phase	Waters ACQUITY UPLC BEH C18 (void)	2025-10-24	56.3
Liquid Chromatography	Reversed-phase	Waters ACQUITY UPLC BEH C18 (void)	2025-10-24	56.3
Liquid Chromatography	Reversed-phase	Waters ACQUITY UPLC BEH C18 (eluted)	2025-10-24	297.7
Liquid Chromatography	Reversed-phase	Waters ACQUITY UPLC BEH C18 (eluted)	2025-10-24	297.7
Liquid Chromatography	Reversed-phase	Kinetex Core-Shell C18 2.6 um, 3.0 x 100 mm, Phenomenex (eluted)	2025-10-24	556.2
Liquid Chromatography	Reversed-phase	Kinetex Core-Shell C18 2.6 um, 3.0 x 100 mm, Phenomenex (eluted)	2025-10-24	556.2
Liquid Chromatography	Reversed-phase	Waters Atlantis T3 (2.1 x 150 mm, 5 um) (eluted)	2025-10-24	537.7
Liquid Chromatography	Reversed-phase	Waters Atlantis T3 (2.1 x 150 mm, 5 um) (eluted)	2025-10-24	537.7

Retention Indices

Chromatography Type	Peak Label	SMILES	Stationary Phase	Deposition Date	Retention Index
Gas Chromatography	3-(Imidazol-4-yl)-2-oxopropyl phosphate_TMS_1	C[Si](C)(C)OP(=O)(O)OCC(=O)CC1=C[NH]C=N1	standard non polar	2025-10-24	1776.69
Gas Chromatography	3-(Imidazol-4-yl)-2-oxopropyl phosphate_TMS_2	C[Si](C)(C)OC(=CC1=C[NH]C=N1)COP(=O)(O)O	standard non polar	2025-10-24	2073.06
Gas Chromatography	3-(Imidazol-4-yl)-2-oxopropyl phosphate_TMS_3	C[Si](C)(C)OC(=COP(=O)(O)O)CC1=C[NH]C=N1	standard non polar	2025-10-24	2383.04
Gas Chromatography	3-(Imidazol-4-yl)-2-oxopropyl phosphate_TMS_4	C[Si](C)(C)N1C=NC(CC(=O)COP(=O)(O)O)=C1	standard non polar	2025-10-24	2289.2
Gas Chromatography	3-(Imidazol-4-yl)-2-oxopropyl phosphate_TMS_5	C[Si](C)(C)OP(=O)(OCC(=O)CC1=C[NH]C=N1)O[Si](C)(C)C	standard non polar	2025-10-24	1988.83
Gas Chromatography	3-(Imidazol-4-yl)-2-oxopropyl phosphate_TMS_6	C[Si](C)(C)OC(=CC1=C[NH]C=N1)COP(=O)(O)O[Si](C)(C)C	standard non polar	2025-10-24	1757.42
Gas Chromatography	3-(Imidazol-4-yl)-2-oxopropyl phosphate_TMS_7	C[Si](C)(C)OC(=COP(=O)(O)O[Si](C)(C)C)CC1=C[NH]C=N1	standard non polar	2025-10-24	2018.83
Gas Chromatography	3-(Imidazol-4-yl)-2-oxopropyl phosphate_TMS_8	C[Si](C)(C)OP(=O)(O)OCC(=O)CC1=CN([Si](C)(C)C)C=N1	standard non polar	2025-10-24	1249.01
Gas Chromatography	3-(Imidazol-4-yl)-2-oxopropyl phosphate_TMS_9	C[Si](C)(C)OC(=CC1=CN([Si](C)(C)C)C=N1)COP(=O)(O)O	standard non polar	2025-10-24	1829.27
Gas Chromatography	3-(Imidazol-4-yl)-2-oxopropyl phosphate_TMS_10	C[Si](C)(C)OC(=COP(=O)(O)O)CC1=CN([Si](C)(C)C)C=N1	standard non polar	2025-10-24	2226.2
Gas Chromatography	3-(Imidazol-4-yl)-2-oxopropyl phosphate_TMS_11	C[Si](C)(C)OC(=CC1=C[NH]C=N1)COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C	standard non polar	2025-10-24	1572.29
Gas Chromatography	3-(Imidazol-4-yl)-2-oxopropyl phosphate_TMS_12	C[Si](C)(C)OC(=COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)CC1=C[NH]C=N1	standard non polar	2025-10-24	1718.99
Gas Chromatography	3-(Imidazol-4-yl)-2-oxopropyl phosphate_TMS_13	C[Si](C)(C)OP(=O)(OCC(=O)CC1=CN([Si](C)(C)C)C=N1)O[Si](C)(C)C	standard non polar	2025-10-24	2161.53
Gas Chromatography	3-(Imidazol-4-yl)-2-oxopropyl phosphate_TMS_14	C[Si](C)(C)OC(=CC1=CN([Si](C)(C)C)C=N1)COP(=O)(O)O[Si](C)(C)C	standard non polar	2025-10-24	2512.92
Gas Chromatography	3-(Imidazol-4-yl)-2-oxopropyl phosphate_TMS_15	C[Si](C)(C)OC(=COP(=O)(O)O[Si](C)(C)C)CC1=CN([Si](C)(C)C)C=N1	standard non polar	2025-10-24	1698.26
Gas Chromatography	3-(Imidazol-4-yl)-2-oxopropyl phosphate_TMS_16	C[Si](C)(C)OC(=CC1=CN([Si](C)(C)C)C=N1)COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C	standard non polar	2025-10-24	1670.43
Gas Chromatography	3-(Imidazol-4-yl)-2-oxopropyl phosphate_TMS_17	C[Si](C)(C)OC(=COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)CC1=CN([Si](C)(C)C)C=N1	standard non polar	2025-10-24	1568.45
Gas Chromatography	3-(Imidazol-4-yl)-2-oxopropyl phosphate_TMS_1	C[Si](C)(C)OP(=O)(O)OCC(=O)CC1=C[NH]C=N1	standard polar	2025-10-24	2081.41
Gas Chromatography	3-(Imidazol-4-yl)-2-oxopropyl phosphate_TMS_2	C[Si](C)(C)OC(=CC1=C[NH]C=N1)COP(=O)(O)O	standard polar	2025-10-24	1969.44
Gas Chromatography	3-(Imidazol-4-yl)-2-oxopropyl phosphate_TMS_3	C[Si](C)(C)OC(=COP(=O)(O)O)CC1=C[NH]C=N1	standard polar	2025-10-24	2381.1
Gas Chromatography	3-(Imidazol-4-yl)-2-oxopropyl phosphate_TMS_4	C[Si](C)(C)N1C=NC(CC(=O)COP(=O)(O)O)=C1	standard polar	2025-10-24	2756.67
Gas Chromatography	3-(Imidazol-4-yl)-2-oxopropyl phosphate_TMS_5	C[Si](C)(C)OP(=O)(OCC(=O)CC1=C[NH]C=N1)O[Si](C)(C)C	standard polar	2025-10-24	2653.39
Gas Chromatography	3-(Imidazol-4-yl)-2-oxopropyl phosphate_TMS_6	C[Si](C)(C)OC(=CC1=C[NH]C=N1)COP(=O)(O)O[Si](C)(C)C	standard polar	2025-10-24	2223.4
Gas Chromatography	3-(Imidazol-4-yl)-2-oxopropyl phosphate_TMS_7	C[Si](C)(C)OC(=COP(=O)(O)O[Si](C)(C)C)CC1=C[NH]C=N1	standard polar	2025-10-24	1833.98
Gas Chromatography	3-(Imidazol-4-yl)-2-oxopropyl phosphate_TMS_8	C[Si](C)(C)OP(=O)(O)OCC(=O)CC1=CN([Si](C)(C)C)C=N1	standard polar	2025-10-24	2646.65
Gas Chromatography	3-(Imidazol-4-yl)-2-oxopropyl phosphate_TMS_9	C[Si](C)(C)OC(=CC1=CN([Si](C)(C)C)C=N1)COP(=O)(O)O	standard polar	2025-10-24	1791.05
Gas Chromatography	3-(Imidazol-4-yl)-2-oxopropyl phosphate_TMS_10	C[Si](C)(C)OC(=COP(=O)(O)O)CC1=CN([Si](C)(C)C)C=N1	standard polar	2025-10-24	2095.85
Gas Chromatography	3-(Imidazol-4-yl)-2-oxopropyl phosphate_TMS_11	C[Si](C)(C)OC(=CC1=C[NH]C=N1)COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C	standard polar	2025-10-24	2205.12
Gas Chromatography	3-(Imidazol-4-yl)-2-oxopropyl phosphate_TMS_12	C[Si](C)(C)OC(=COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)CC1=C[NH]C=N1	standard polar	2025-10-24	2182.41
Gas Chromatography	3-(Imidazol-4-yl)-2-oxopropyl phosphate_TMS_13	C[Si](C)(C)OP(=O)(OCC(=O)CC1=CN([Si](C)(C)C)C=N1)O[Si](C)(C)C	standard polar	2025-10-24	1379.05
Gas Chromatography	3-(Imidazol-4-yl)-2-oxopropyl phosphate_TMS_14	C[Si](C)(C)OC(=CC1=CN([Si](C)(C)C)C=N1)COP(=O)(O)O[Si](C)(C)C	standard polar	2025-10-24	1907.87
Gas Chromatography	3-(Imidazol-4-yl)-2-oxopropyl phosphate_TMS_15	C[Si](C)(C)OC(=COP(=O)(O)O[Si](C)(C)C)CC1=CN([Si](C)(C)C)C=N1	standard polar	2025-10-24	2239.29
Gas Chromatography	3-(Imidazol-4-yl)-2-oxopropyl phosphate_TMS_16	C[Si](C)(C)OC(=CC1=CN([Si](C)(C)C)C=N1)COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C	standard polar	2025-10-24	2521.12
Gas Chromatography	3-(Imidazol-4-yl)-2-oxopropyl phosphate_TMS_17	C[Si](C)(C)OC(=COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)CC1=CN([Si](C)(C)C)C=N1	standard polar	2025-10-24	1080.12

Biological Properties

Cellular Locations

Not Available

Biospecimen Locations

Feces

Tissue Locations

Not Available

Associated OMIM IDs

114500 (Colorectal cancer)
610247 (Eosinophilic esophagitis)

Human Proteins and Enzymes

Protein ID	Protein Name	Protein Type	Uniprot ID	Species

Human Pathways

Pathways

Name	SMPDB/PathBank

Microbial Pathways

Pathways

Not Available

Metabolic Reactions

Reactions

This table shows at most 20 reactions. For the full list of associated reactions:

See All Associated Reactions

Reaction ID	Precursor	Product	Enzyme	Reaction Type	Data Source	Reference

Health Effects and Bioactivity

Health Outcome/Bioactivity	Metabolite Response/Effect	Evidence Type	Host and Biospecimen	Data Source	Reference

Microbial Sources

Superkingdom/Kingdom	Phylum	Total species	Hosts and Body Sites	Microbial Links
Bacteria/Eubacteria	Firmicutes	354	Human feces; Human pleural fluid plaque; Pig ; Human ; Human subgingival plaque; Catfish ; Cattle	Metabolic reconstruction
Bacteria/Eubacteria	Proteobacteria	480	Human feces; Human sputum; Human ; Human unknown; Pig ; Human pleural fluid plaque; Human dental plaque; Human nasal swab; Human feces; pleural fluid plaque; bal; Cattle ; Turkey ; Sheep ; Chicken ; River trout	Metabolic reconstruction
Bacteria/Eubacteria	Actinobacteria	159	Human feces; Human pleural fluid plaque; Human dental plaque; Human sputum; Human ; Human supragingival plaque; Human mucosa; Human subgingival plaque; Cattle	Metabolic reconstruction
Bacteria/Eubacteria	Verrucomicrobia	2	Human ; Human feces	Metabolic reconstruction
Bacteria/Eubacteria	Bacteroidetes	101	Human feces; Human appendix biopsy; Human ; Human urine; Human gastric fluid; Human saliva; Human supragingival plaque; Human subgingival plaque	Metabolic reconstruction
Bacteria/Eubacteria	Synergistetes	3	Human feces	Metabolic reconstruction
Archaea	Thaumarchaeota	1		Metabolic reconstruction
Bacteria	Firmicutes	2	Human feces; Human pleural fluid plaque; Pig ; Human ; Human subgingival plaque; Catfish ; Cattle	Metabolic reconstruction
Archaea	Euryarchaeota	5		Metabolic reconstruction
Bacteria/Eubacteria	Fusobacteria	1	Human ; Human feces	Metabolic reconstruction
Eukaryota/Fungi	Ascomycota	20	Human feces; Human saliva; Human supragingival plaque	Metabolic reconstruction
Bacteria/Eubacteria	Planctomycetes	2	Human feces	Metabolic reconstruction
Archaea	Crenarchaeota	1		Metabolic reconstruction
Bacteria	Synergistetes	1	Human feces	Metabolic reconstruction
Bacteria	Proteobacteria	7	Human feces; Human sputum; Human ; Human unknown; Pig ; Human pleural fluid plaque; Human dental plaque; Human nasal swab; Human feces; pleural fluid plaque; bal; Cattle ; Turkey ; Sheep ; Chicken ; River trout	Metabolic reconstruction
Bacteria/Eubacteria	Aquificae	3
Archaea/Archaea	Euryarchaeota	30		Metabolic reconstruction
Archaea/Archaea	Crenarchaeota	13		Metabolic reconstruction
Archaea/Archaea	Thaumarchaeota	1		Metabolic reconstruction
Bacteria/Eubacteria	Chloroflexi	7
Bacteria/Eubacteria	Chlorobi	11
Eukaryota/Fungi	Basidiomycota	3	Human feces
Bacteria/Eubacteria	Deinococcus-thermus	5
Bacteria/Eubacteria	Dictyoglomi	2
Bacteria/Eubacteria	Elusimicrobia	1
Bacteria/Eubacteria	Cyanobacteria	31	Human
Bacteria/Eubacteria	Acidobacteria	2
Bacteria/Eubacteria	Spirochaetes	7	Human ; Pig
Bacteria	nah	1
Bacteria/Eubacteria	Thermotogae	4
Bacteria/Eubacteria	Nitrospirae	1

Exposure Sources

Other Exposures

Source Type	Data Source	Reference

Host Biospecimen and Location

Host and Biospecimen	Status	Mean	Std	Min	Max	Units	Age	Sex	Health Condition	Data Source	Reference
Human Feces	Detected but not Quantified									HMDB

External Links

HMDB ID

HMDB0012236

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

KNApSAcK ID

Chemspider ID

KEGG Compound ID

BioCyc ID

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

792

PDB ID

Not Available

ChEBI ID

16426

Food Biomarker Ontology

Not Available

CMMC Knowledgebase

Not Available

General References

Henderson GB, Snell EE: Vitamin B 6 -responsive histidine deficiency in mutants of Salmonella typhimurium. Proc Natl Acad Sci U S A. 1971 Dec;68(12):2903-7. doi: 10.1073/pnas.68.12.2903. [PubMed:4943547 ]
Albritton WL, Levin AP: Some comparative kinetic data on the enzyme imidazoleacetol phosphate:L-glutamate aminotransferase derived from mutant strains of Salmonella typhimurium. J Biol Chem. 1970 May 25;245(10):2525-8. [PubMed:5445798 ]
AMES BN, HORECKER BL: The biosynthesis of histidine: imidazoleacetol phosphate transaminase. J Biol Chem. 1956 May;220(1):113-28. [PubMed:13319331 ]
LEVIN AP, HARTMAN PE: ACTION OF A HISTIDINE ANALOGUE, 1,2,4-TRIAZOLE-3-ALANINE, IN SALMONELLA TYPHIMURIUM. J Bacteriol. 1963 Oct;86:820-8. doi: 10.1128/jb.86.4.820-828.1963. [PubMed:14066480 ]
AMES BN, MITCHELL HK: The biosynthesis of histidine; imidazoleglycerol phosphate, imidazoleacetol phosphate, and histidinol phosphate. J Biol Chem. 1955 Feb;212(2):687-96. [PubMed:14353870 ]

Showing metabocard for 3-(Imidazol-4-yl)-2-oxopropyl phosphate (MMDBc0049988)

MOL for #<Metabolite:0x00007f9acd34ec38>

3D MOL for #<Metabolite:0x00007f9acd34ec38>

3D SDF for #<Metabolite:0x00007f9acd34ec38>

3D-SDF for #<Metabolite:0x00007f9acd34ec38>

PDB for #<Metabolite:0x00007f9acd34ec38>

3D PDB for #<Metabolite:0x00007f9acd34ec38>

SMILES for #<Metabolite:0x00007f9acd34ec38>

INCHI for #<Metabolite:0x00007f9acd34ec38>

Structure for #<Metabolite:0x00007f9acd34ec38>

3D Structure for #<Metabolite:0x00007f9acd34ec38>